Merck to Present New HIV Treatment and Prevention Data at European AIDS Conference 2025

Reuters

Oct 09

Merck to Present New HIV Treatment and Prevention Data at European AIDS Conference 2025

Merck & Co. Inc. announced that it will present new data from its HIV treatment and prevention pipeline at the 20th European AIDS Conference (EACS 2025), scheduled for October 15-18, 2025, in Paris, France. Planned presentations include an oral presentation on weight and body composition at Week 48 from a Phase 3 trial comparing doravirine/islatravir (DOR/ISL) to bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) for adults with virologically suppressed HIV-1 infection. Additional data to be presented include fasting lipids and insulin resistance from two Phase 3 trials, 96-week safety and pharmacokinetics from a Phase 2 trial of once-weekly islatravir/lenacapavir, and Phase 1 safety and pharmacokinetics of the investigational once-monthly PrEP pill MK-8527 in adults with renal impairment. These results will be presented at the upcoming conference.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Merck & Co. Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251009184957) on October 09, 2025, and is solely responsible for the information contained therein.

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Inc. announced that it will present new data from its HIV treatment and prevention pipeline at the 20th European AIDS Conference (EACS 2025), scheduled for October 15-18, 2025, in Paris, France. Planned presentations include an oral presentation on weight and body composition at Week 48 from a Phase 3 trial comparing doravirine/islatravir (DOR/ISL) to bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) for adults with virologically suppressed HIV-1 infection. Additional data to be presented include fasting lipids and insulin resistance from two Phase 3 trials, 96-week safety and pharmacokinetics from a Phase 2 trial of once-weekly islatravir/lenacapavir, and Phase 1 safety and pharmacokinetics of the investigational once-monthly PrEP pill MK-8527 in adults with renal impairment. These results will be presented at the upcoming conference.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. 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